ENST00000470094.2:c.9137T>G
|
ENSP00000434898.2:p.Phe3046Cys
|
|
ENST00000528762.2:c.*504T>G
|
ENSP00000433168.2:n.*504T>G
|
|
ENST00000530893.7:c.8768T>G
|
ENSP00000499438.2:p.Phe2923Cys
|
|
ENST00000665585.2:c.*699T>G
|
ENSP00000499570.2:n.*699T>G
|
|
ENST00000666593.2:c.9137T>G
|
ENSP00000499256.2:p.Phe3046Cys
|
|
ENST00000700202.2:c.9086T>G
|
ENSP00000514856.2:p.Phe3029Cys
|
|
ENST00000700202.1:c.1553T>G
|
ENSP00000514856.1:p.Phe518Cys
|
|
ENST00000700203.1:n.1264T>G
|
|
|
ENST00000380152.8:c.9137T>G
MANE Select
|
ENSP00000369497.3:p.Phe3046Cys
|
|
ENST00000544455.6:c.9137T>G
|
ENSP00000439902.1:p.Phe3046Cys
|
|
ENST00000614259.2:c.9145T>G
|
ENSP00000506251.1:n.9145T>G
|
|
ENST00000665585.1:c.2015T>G
|
|
|
ENST00000666593.1:c.20T>G
|
ENSP00000499256.1:p.Phe7Cys
|
|
ENST00000680887.1:c.9137T>G
|
ENSP00000505508.1:p.Phe3046Cys
|
|
ENST00000380152.7:c.9137T>G
|
ENSP00000369497.3:p.Phe3046Cys
|
|
ENST00000470094.1:c.94T>G
|
|
|
ENST00000544455.5:c.9137T>G
|
ENSP00000439902.1:p.Phe3046Cys
|
|
NM_000059.3:c.9137T>G , LRG_293t1:c.9137T>G
|
NP_000050.2:p.Phe3046Cys
|
|
XM_011535203.1:c.9137T>G
|
XP_011533505.1:p.Phe3046Cys
|
|
XM_011535204.1:c.9041T>G
|
XP_011533506.1:p.Phe3014Cys
|
|
NM_000059.4:c.9137T>G
MANE Select
|
NP_000050.3:p.Phe3046Cys
|
|